121 related articles for article (PubMed ID: 8886006)
1. CFTR expression in C127 cells is associated with enhanced cell shrinkage and ATP extrusion in Cl(-)-free medium.
Rotoli BM; Bussolati O; Dall' Asta V; Hoffmann EK; Cabrini G; Gazzola GC
Biochem Biophys Res Commun; 1996 Oct; 227(3):755-61. PubMed ID: 8886006
[TBL] [Abstract][Full Text] [Related]
2. Swelling-activated, cystic fibrosis transmembrane conductance regulator-augmented ATP release and Cl- conductances in murine C127 cells.
Hazama A; Fan HT; Abdullaev I; Maeno E; Tanaka S; Ando-Akatsuka Y; Okada Y
J Physiol; 2000 Feb; 523 Pt 1(Pt 1):1-11. PubMed ID: 10673540
[TBL] [Abstract][Full Text] [Related]
3. Expression of cystic fibrosis transmembrane conductance regulator alters the responses to hypotonic cell swelling and ATP of Chinese hamster ovary cells.
Thiele IE; Hug MJ; Hübner M; Greger R
Cell Physiol Biochem; 1998; 8(1-2):61-74. PubMed ID: 9547020
[TBL] [Abstract][Full Text] [Related]
4. Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.
Poulsen JH; Fischer H; Illek B; Machen TE
Proc Natl Acad Sci U S A; 1994 Jun; 91(12):5340-4. PubMed ID: 7515498
[TBL] [Abstract][Full Text] [Related]
5. Mutant cystic fibrosis transmembrane conductance regulator inhibits acidification and apoptosis in C127 cells: possible relevance to cystic fibrosis.
Gottlieb RA; Dosanjh A
Proc Natl Acad Sci U S A; 1996 Apr; 93(8):3587-91. PubMed ID: 8622979
[TBL] [Abstract][Full Text] [Related]
6. Changes in neutral amino acid efflux and membrane potential associated with the expression of CFTR protein.
Rotoli BM; Bussolati O; Cabrini G; Gazzola GC
Amino Acids; 1996 Jun; 11(2):247-55. PubMed ID: 24178690
[TBL] [Abstract][Full Text] [Related]
7. CFTR protein is involved in the efflux of neutral amino acids.
Rotoli BM; Bussolati O; Sironi M; Cabrini G; Gazzola GC
Biochem Biophys Res Commun; 1994 Oct; 204(2):653-8. PubMed ID: 7526852
[TBL] [Abstract][Full Text] [Related]
8. Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression.
Cheng SH; Fang SL; Zabner J; Marshall J; Piraino S; Schiavi SC; Jefferson DM; Welsh MJ; Smith AE
Am J Physiol; 1995 Apr; 268(4 Pt 1):L615-24. PubMed ID: 7733303
[TBL] [Abstract][Full Text] [Related]
9. Multiple intracellular pathways for regulation of chloride secretion in cultured pig tracheal submucosal gland cells.
Zhang AL; Roomans GM
Eur Respir J; 1999 Mar; 13(3):571-6. PubMed ID: 10232428
[TBL] [Abstract][Full Text] [Related]
10. Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein.
Brown CR; Hong-Brown LQ; Biwersi J; Verkman AS; Welch WJ
Cell Stress Chaperones; 1996 Jun; 1(2):117-25. PubMed ID: 9222597
[TBL] [Abstract][Full Text] [Related]
11. The cystic fibrosis transmembrane conductance regulator is an extracellular chloride sensor.
Broadbent SD; Ramjeesingh M; Bear CE; Argent BE; Linsdell P; Gray MA
Pflugers Arch; 2015 Aug; 467(8):1783-94. PubMed ID: 25277268
[TBL] [Abstract][Full Text] [Related]
12. 8-cyclopentyl-1,3-dipropylxanthine and other xanthines differentially bind to the wild-type and delta F508 first nucleotide binding fold (NBF-1) domains of the cystic fibrosis transmembrane conductance regulator.
Cohen BE; Lee G; Jacobson KA; Kim YC; Huang Z; Sorscher EJ; Pollard HB
Biochemistry; 1997 May; 36(21):6455-61. PubMed ID: 9174362
[TBL] [Abstract][Full Text] [Related]
13. Mutation of R555 in CFTR-delta F508 enhances function and partially corrects defective processing.
Teem JL; Carson MR; Welsh MJ
Recept Channels; 1996; 4(1):63-72. PubMed ID: 8723647
[TBL] [Abstract][Full Text] [Related]
14. External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism.
Cantiello HF; Prat AG; Reisin IL; Ercole LB; Abraham EH; Amara JF; Gregory RJ; Ausiello DA
J Biol Chem; 1994 Apr; 269(15):11224-32. PubMed ID: 7512560
[TBL] [Abstract][Full Text] [Related]
15. Protein kinase C activates chloride conductance in C127 cells stably expressing the cystic fibrosis gene.
Dechecchi MC; Tamanini A; Berton G; Cabrini G
J Biol Chem; 1993 May; 268(15):11321-5. PubMed ID: 7684379
[TBL] [Abstract][Full Text] [Related]
16. Genistein potentiates wild-type and delta F508-CFTR channel activity.
Hwang TC; Wang F; Yang IC; Reenstra WW
Am J Physiol; 1997 Sep; 273(3 Pt 1):C988-98. PubMed ID: 9316420
[TBL] [Abstract][Full Text] [Related]
17. cAMP and genistein stimulate HCO3- conductance through CFTR in human airway epithelia.
Illek B; Yankaskas JR; Machen TE
Am J Physiol; 1997 Apr; 272(4 Pt 1):L752-61. PubMed ID: 9142951
[TBL] [Abstract][Full Text] [Related]
18. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive.
Denning GM; Anderson MP; Amara JF; Marshall J; Smith AE; Welsh MJ
Nature; 1992 Aug; 358(6389):761-4. PubMed ID: 1380673
[TBL] [Abstract][Full Text] [Related]
19. In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR.
Rubenstein RC; Egan ME; Zeitlin PL
J Clin Invest; 1997 Nov; 100(10):2457-65. PubMed ID: 9366560
[TBL] [Abstract][Full Text] [Related]
20. Diffusional mobility of the cystic fibrosis transmembrane conductance regulator mutant, delta F508-CFTR, in the endoplasmic reticulum measured by photobleaching of GFP-CFTR chimeras.
Haggie PM; Stanton BA; Verkman AS
J Biol Chem; 2002 May; 277(19):16419-25. PubMed ID: 11877404
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]